Article
Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis.
Human molecular genetics - 15 Feb 2009
Baranzini Sergio E, Wang Joanne, Gibson Rachel A, Galwey Nicholas, Naegelin Yvonne, Barkhof Frederik, Radue Ernst-Wilhelm, Lindberg Raija L P, Uitdehaag Bernard M G, Johnson Michael R, Angelakopoulou Aspasia, Hall Leslie, Richardson Jill C, Prinjha Rab K, Gass Achim, Geurts Jeroen J G, Kragt Jolijn, Sombekke Madeleine, Vrenken Hugo, Qualley Pamela, Lincoln Robin R, Gomez Refujia, Caillier Stacy J, George Michaela F, Mousavi Hourieh, Guerrero Rosa, Okuda Darin T, Cree Bruce A C, Green Ari J, Waubant Emmanuelle, Goodin Douglas S, Pelletier Daniel, Matthews Paul M, Hauser Stephen L, Kappos Ludwig, Polman Chris H, Oksenberg Jorge R
Abstract excerpt
Multiple sclerosis (MS), a chronic disorder of the central nervous system and common cause of neurological disability in young adults, is characterized by moderate but complex risk heritability. Here we report the results of a genome-wide association study performed in a 1000 prospective case ser...
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